HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 3-[2-(Pyridin-2-ylamino)thiazol-5-ylmethylsulfanyl]benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzoic acid, 3-mercapto- | HCID 95737 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | (5-Chloromethylthiazol-2-yl)pyridin-2-ylamine hydrochloride | HCID 86591883 | — |
| Product | 3-[2-(Pyridin-2-ylamino)thiazol-5-ylmethylsulfanyl]benzoic acid | HCID 22019055 | — |
Reaction Steps
A mixture of 3-mercaptobenzoic acid (308 mg, 2 mmol) and sodium hydride (60% in oil, 160 mg, 4 mmol) was stirred at RT under argon for 10 min and then cooled to 0° C. and (5-chloromethyl-thiazol-2-yl)pyridin-2-yl-amine hydrochloride salt (262 mg, 1 mmol) was added. The resulting reaction mixture was stirred at 0° C. for 1 h and acidified with 1N potassium hydrogen sulfate solution to pH=4. The mixture was filtered and the collected solid was washed with water and dried in vacuo to provide compound 11A, 3-[2-(pyridin-2-ylamino)thiazol-5-ylmethylsulfanyl]benzoic acid, which was used directly for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07547711B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-116bbf57ff314b3aaa67164b0336632c |
| Source note | uspto-grants-2009_06 |